Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_provenance.
- NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_assertion description "[We describe the detection of a novel missense mutation (Thr176-->Ile) that is located at the neo N-terminus of activated protein C. The Thr176-->Ile substitution leads to a type 1 deficiency state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_provenance.
- NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_assertion evidence source_evidence_literature NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_provenance.
- NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_assertion SIO_000772 7705844 NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_provenance.
- NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_assertion wasDerivedFrom befree-2016 NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_provenance.
- NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_assertion wasGeneratedBy ECO_0000203 NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1319077.RA7NVhSjXGFYlVcrBsJ2Zx2riPMX2vtvmHGsYwd6V9hP8130_provenance.