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- source_evidence_literature type ECO_0000212 NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_provenance.
- NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_assertion description "[Maternal CVT has been associated with factor V Leiden, the prothrombin G20210A mutation, protein C deficiency and hyperhomocysteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_provenance.
- NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_assertion evidence source_evidence_literature NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_provenance.
- NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_assertion SIO_000772 23337711 NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_provenance.
- NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_assertion wasDerivedFrom befree-20150227 NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_provenance.
- NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_assertion wasGeneratedBy ECO_0000203 NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP391767.RA1hfXz28A4PhiTRAMSgP90tU0THUHIxElLhIp7sWKAQ8130_provenance.