Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_provenance.
- NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_assertion description "[However, we identified rare variants in ENG and TGFBR3 that may be important for IA pathogenesis in a subset of families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_provenance.
- NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_assertion evidence source_evidence_literature NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_provenance.
- NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_assertion SIO_000772 19299629 NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_provenance.
- NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_assertion wasDerivedFrom befree-20150227 NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_provenance.
- NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_assertion wasGeneratedBy ECO_0000203 NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP734662.RAGACQ1JGEIkuic-7AR3m241WI4JudJRXKoD0m3CJcLaI130_provenance.