Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_provenance.
- NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_assertion description "[Factor V Leiden gene (most common) and the prothrombin G20210A gene mutation are inherited mild to moderate risk factors for hypercoagulability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_provenance.
- NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_assertion evidence source_evidence_literature NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_provenance.
- NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_assertion SIO_000772 17721328 NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_provenance.
- NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_assertion wasDerivedFrom befree-2016 NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_provenance.
- NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_assertion wasGeneratedBy ECO_0000203 NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_provenance.
- befree-2016 importedOn "2016-02-19" NP626703.RAIkHNG2Rq-rnjKwTSy4kbjd2M9OtuLgHHsT5yI820qFI130_provenance.