Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_provenance.
- NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_assertion description "[All participants had a thrombotic workup that included the following: genetic markers: factor V Leiden G1691A and G20210A prothrombin mutations, methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms; protein assays: protein C, protein S and antithrombin; other tests: blood typing and screening for hyperhomocysteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_provenance.
- NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_assertion evidence source_evidence_literature NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_provenance.
- NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_assertion SIO_000772 23337711 NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_provenance.
- NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_assertion wasDerivedFrom befree-20150227 NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_provenance.
- NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_assertion wasGeneratedBy ECO_0000203 NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP640898.RAqcYw13sxrSkRfJmuP1db8E-8Cy4IqMfGQySc68wEGUs130_provenance.