Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_provenance.
- NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_assertion description "[Together, these results indicate that lack of necdin during development likely contributes to the hypogonadotrophic hypogonadal phenotype in individuals with PWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_provenance.
- NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_assertion evidence source_evidence_literature NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_provenance.
- NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_assertion SIO_000772 18930956 NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_provenance.
- NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_assertion wasDerivedFrom befree-20140225 NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_provenance.
- NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_assertion wasGeneratedBy ECO_0000203 NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP400059.RAxU1AA5iU1L5RP2lnTR4qJ9-xtmZTYWiEAc3f101ZxlE130_provenance.