Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_provenance.
- NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_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." NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_provenance.
- NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_assertion evidence source_evidence_literature NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_provenance.
- NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_assertion SIO_000772 17718864 NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_provenance.
- NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_assertion wasDerivedFrom lhgdn-20090331 NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_provenance.
- NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_assertion wasGeneratedBy ECO_0000203 NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP139879.RAKyyvbcHXZNGoa8MZH2Fw04oRgcRsqj_U3gBXGCuHjwI130_provenance.