Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_provenance.
- NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_assertion description "[VACTERL with hydrocephalus in twins due to Fanconi anemia (FA): mutation in the FAC gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_provenance.
- NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_assertion evidence source_evidence_literature NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_provenance.
- NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_assertion SIO_000772 8986283 NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_provenance.
- NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_assertion wasDerivedFrom befree-2016 NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_provenance.
- NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_assertion wasGeneratedBy ECO_0000203 NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1365183.RActYc5s3gfmF3-jXqXyvsVLPpxPm3o69cMfq-JavEvGk130_provenance.