Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance.
- NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_assertion wasGeneratedBy ECO_0000203 NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance.
- NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_assertion wasDerivedFrom befree-20140225 NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance.
- NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_assertion SIO_000772 17018384 NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance.
- NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_assertion evidence source_evidence_literature NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance.
- NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_assertion description "[Glanzmann thrombasthenia is an autosomal recessive bleeding disorder characterized by a life-long hemorrhagic tendency and absent or severely reduced platelet aggregation in response to agonists, caused by quantitative or qualitative abnormalities in the platelet fibrinogen receptor, integrin alphaIIb beta3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance.