Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_provenance.
- NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_assertion description "[Defective function of glucose-6-phosphatase, catalytic subunit 3, underlies a severe congenital neutropenia syndrome associated with cardiac and urogenital malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_provenance.
- NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_assertion evidence source_evidence_literature NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_provenance.
- NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_assertion SIO_000772 19118303 NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_provenance.
- NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_assertion wasDerivedFrom lhgdn-20090331 NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_provenance.
- NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_assertion wasGeneratedBy ECO_0000203 NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP244782.RAO3f7S82h1OGTQ0yswnChxQLdMuZatRBBGUvvpPB1IFo130_provenance.