Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_provenance.
- NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_assertion wasGeneratedBy ECO_0000203 NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_provenance.
- NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_assertion wasDerivedFrom befree-20140225 NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_provenance.
- NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_assertion SIO_000772 8855829 NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_provenance.
- NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_assertion evidence source_evidence_literature NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_provenance.
- NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_assertion description "[The recent finding that a mutation in the FSH receptor gene causes ovarian dysgenesis prompted the present study to determine the phenotype caused by this mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP704030.RA4DIS0dd1VfhvvL-7zUZwE_880PnzULxeEkRwc4TtrMA130_provenance.