Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_provenance.
- NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_assertion description "[Heterozygous mutations in the type II collagen gene (COL2A1) result in a group of skeletal dysplasias known as Type II collagenopathy (COL2pathy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_provenance.
- NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_assertion evidence source_evidence_literature NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_provenance.
- NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_assertion SIO_000772 25187577 NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_provenance.
- NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_assertion wasDerivedFrom befree-2016 NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_provenance.
- NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_assertion wasGeneratedBy ECO_0000203 NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216702.RAI69g-oyfO7cw8jdV4KGk9lSrmVePkkUTGXylelCnSww130_provenance.