Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance.
- NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_assertion wasGeneratedBy ECO_0000203 NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance.
- NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_assertion wasDerivedFrom befree-20140225 NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance.
- NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_assertion SIO_000772 8308926 NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance.
- NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_assertion evidence source_evidence_literature NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance.
- NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_assertion description "[Germline p53 gene mutations were detected in six of 19 patients with multifocal glioma, including two with family history of cancer, one with another primary malignancy, and two with all three risk factors; one of four patients with unifocal glioma, another primary malignancy, and a family history of cancer; and two of 15 patients with unifocal glioma and a family history of cancer but no second malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance.