Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion> ?p ?o ?g. }
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- NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion type Assertion NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_head.
- 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.
- NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion evidence source_evidence_literature NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion SIO_000772 23000143 NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion wasDerivedFrom befree-2016 NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.
- NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_assertion wasGeneratedBy ECO_0000203 NP1015007.RAoppfY9ZLKEy0iQGcfgIxYL67vuvkZzqOUC3SIREMPXc130_provenance.