Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_provenance.
- NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_assertion description "[Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_provenance.
- NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_assertion evidence source_evidence_literature NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_provenance.
- NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_assertion SIO_000772 20587610 NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_provenance.
- NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_assertion wasDerivedFrom gad-20130706 NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_provenance.
- NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_assertion wasGeneratedBy ECO_0000203 NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_provenance.
- gad-20130706 importedOn "2013-07-06" NP86491.RAoSut3S-WzjiQh2WhpGpDLjtCN--BV7aRlSFxS_8bk4M130_provenance.