Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_provenance.
- NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_assertion description "[Mutations in CYP1B1 account for approximately one in five primary congenital glaucoma cases from Australia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_provenance.
- NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_assertion evidence source_evidence_literature NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_provenance.
- NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_assertion SIO_000772 17718864 NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_provenance.
- NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_assertion wasDerivedFrom lhgdn-20090331 NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_provenance.
- NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_assertion wasGeneratedBy ECO_0000203 NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP203026.RArZfSa8I5PvkKwoc1Ei9WHdRSYRO8-uik-osSHRUv8DU130_provenance.