Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion description "[The conclusion that most variants of OI are caused by mutations in the structural genes for type I procollagen has broad implications for other diseases that affect connective tissue, diseases such as chondrodystrophies, osteoarthritis, and osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion evidence source_evidence_literature NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion SIO_000772 2683782 NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion wasDerivedFrom befree-20140225 NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_assertion wasGeneratedBy ECO_0000203 NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP511307.RA4KsXr7h0AbmNkOHAXksyianMwqXm25rOxUmzVCnF2TE130_provenance.