Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_provenance.
- NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_assertion description "[Mutation screening of 67 females with idiopathic POF identified a third patient with a missense mutation (H165R) located in the cytochrome b5 domain of PGRMC1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_provenance.
- NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_assertion evidence source_evidence_literature NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_provenance.
- NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_assertion SIO_000772 18782852 NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_provenance.
- NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_assertion wasDerivedFrom befree-20140225 NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_provenance.
- NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_assertion wasGeneratedBy ECO_0000203 NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP301096.RA_t2sLEQ1_9m4wnZ5HXpCd2ovUechtizOINnLoin2DLw130_provenance.