Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_provenance.
- NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_assertion description "[Recent evidence shows that NPS is the result of mutations in the LIM-homeodomain gene LMX1B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_provenance.
- NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_assertion evidence source_evidence_literature NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_provenance.
- NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_assertion SIO_000772 9837817 NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_provenance.
- NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_assertion wasDerivedFrom befree-20150227 NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_provenance.
- NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_assertion wasGeneratedBy ECO_0000203 NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_provenance.
- befree-20150227 importedOn "2015-02-27" NP848704.RAcibbeWqvtv1aZ0UwPkHihK8itQ1Xpomh3sfOsHIRYco130_provenance.