Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_provenance.
- NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_assertion description "[The majority of CMDs therefore arise as the result of either a deficiency of laminin-?2 (MDC1A) or hypoglycosylation of ?-dystroglycan (dystroglycanopathy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_provenance.
- NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_assertion evidence source_evidence_literature NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_provenance.
- NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_assertion SIO_000772 25449259 NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_provenance.
- NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_assertion wasDerivedFrom befree-2016 NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_provenance.
- NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_assertion wasGeneratedBy ECO_0000203 NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_provenance.
- befree-2016 importedOn "2016-02-19" NP1242444.RArTnTo--WKKMQvZQR9oIqmVEL-BrsPTvBXK_Tb-NwI24130_provenance.