Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_provenance.
- NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_assertion description "[Factor VIII-von Willebrand factor binding defects in autosomal recessive von Willebrand disease type Normandy and in mild hemophilia A. New insights into factor VIII-von Willebrand factor interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_provenance.
- NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_assertion evidence source_evidence_literature NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_provenance.
- NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_assertion SIO_000772 19506355 NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_provenance.
- NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_assertion wasDerivedFrom befree-20140225 NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_provenance.
- NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_assertion wasGeneratedBy ECO_0000203 NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP272087.RAk8MNSWFk5IdmUCArXm9XCYChuEu2b6rkVo9Ya1Sbi4s130_provenance.