Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_provenance.
- NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_assertion description "[A total absence of FVIII:C has never been reported in type 3 VWD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_provenance.
- NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_assertion evidence source_evidence_literature NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_provenance.
- NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_assertion SIO_000772 19563498 NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_provenance.
- NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_assertion wasDerivedFrom befree-20140225 NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_provenance.
- NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_assertion wasGeneratedBy ECO_0000203 NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP287435.RA641Vyd-I5ObIAB5ZTepPKE7HX4UkKBgTxkcYNheD3cs130_provenance.