Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion description "[A deletion of Asn169 in the peripherin/RDS protein causes a peculiar form of autosomal dominant macular dystrophy in a large family from the Netherlands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion evidence source_evidence_literature NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion SIO_000772 14557182 NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion wasDerivedFrom befree-20150227 NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_assertion wasGeneratedBy ECO_0000203 NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP668605.RAWW0d8ZKfdKcv_EgPmagjXXFAsc_ArjM2ah2ia8kJU7U130_provenance.