Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion wasGeneratedBy ECO_0000203 NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion wasDerivedFrom befree-2016 NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion SIO_000772 23000143 NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion evidence source_evidence_literature NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion description "[A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.