http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#head
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#assertion
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#provenance
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#assertion
http://rdf.disgenet.org/resource/gda/DGNf291e8cfe85d1f115cd45e5ef27e1896
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/120892
http://rdf.disgenet.org/resource/gda/DGNf291e8cfe85d1f115cd45e5ef27e1896
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0030567
http://rdf.disgenet.org/resource/gda/DGNf291e8cfe85d1f115cd45e5ef27e1896
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001121
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#provenance
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#assertion
http://purl.org/dc/terms/description
[Although it has yet to be proven conclusively that variants in LRRK1 are indeed causative of PD, our data strengthen a possible role for LRRK1 in addition to LRRK2 in the genetic underpinnings of PD but, at the same time, highlight the difficulties encountered in the study of rare variants identified by next-generation sequencing in diseases with autosomal dominant or complex patterns of inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#assertion
http://purl.org/ontology/wi/core#evidence
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/24241507
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://purl.org/pav/importedOn
2017-02-19
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.obolibrary.org/obo/ECO_0000212
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#comment
Gene-disease associations inferred from text-mining the literature.
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#label
DisGeNET evidence - LITERATURE
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/dc/terms/created
2017-10-17T13:19:04+02:00
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1400355.RAHvlSULhukLfC_rcsPOYm_18StbqBp_ILZAYar-xzN_s
http://purl.org/pav/version
v5.0.0.0
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://purl.org/pav/version
v5.0.0