Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion description "[Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion evidence source_evidence_literature NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion SIO_000772 15389319 NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion wasDerivedFrom befree-20150227 NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_assertion wasGeneratedBy ECO_0000203 NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP873849.RAOJvUvxuPpMXKbEpFXe4W5GaxT-LVVYylu_Bs0xEx07M130_provenance.