Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion evidence source_evidence_literature NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion SIO_000772 11030761 NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion wasDerivedFrom befree-2016 NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion wasGeneratedBy ECO_0000203 NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.
- befree-2016 importedOn "2016-02-19" NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.