Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_provenance.
- befree-2016 importedOn "2016-02-19" NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_provenance.
- NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_assertion wasGeneratedBy ECO_0000203 NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_provenance.
- NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_assertion wasDerivedFrom befree-2016 NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_provenance.
- NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_assertion SIO_000772 12619114 NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_provenance.
- NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_assertion evidence source_evidence_literature NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_provenance.
- NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_assertion description "[Specific emphasis is placed on genetic alterations and the prevalence of TP53 (p53) gene alterations in the distinct biological ovarian tumors (benign, borderline, and malignant) and histological subtypes (serous, mucinous, endometrioid, clear cell), as well as in BRCA1-associated hereditary ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP385855.RAwScJUU_KEjZlbFpv98_noJW7tOeD7ZabrTaipQwlFhU130_provenance.