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- source_evidence_literature type ECO_0000212 NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_provenance.
- NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_assertion description "[Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_provenance.
- NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_assertion evidence source_evidence_literature NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_provenance.
- NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_assertion SIO_000772 12920067 NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_provenance.
- NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_assertion wasDerivedFrom befree-2016 NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_provenance.
- NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_assertion wasGeneratedBy ECO_0000203 NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_provenance.
- befree-2016 importedOn "2016-02-19" NP405675.RAbumjQoZp_izO1PpkT7hiUo8RfoQXkMR3JPYn1iAZXRM130_provenance.