Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_provenance.
- NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_assertion description "[An array of vastly different diagnoses is caused by similar mutations in FGFR3, including syndromes affecting skeletal development (hypochondroplasia [HCH], ACH, thanatophoric dysplasia [TD]), skin (epidermal nevi, seborrhaeic keratosis, acanthosis nigricans), and cancer (multiple myeloma [MM], prostate and bladder carcinoma, seminoma).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_provenance.
- NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_assertion evidence source_evidence_literature NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_provenance.
- NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_assertion SIO_000772 22045636 NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_provenance.
- NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_assertion wasDerivedFrom befree-20140225 NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_provenance.
- NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_assertion wasGeneratedBy ECO_0000203 NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP467306.RA0HrHASOnoXmazWnSn6HPBwi2KsN0igBm3CsMQIMrPPs130_provenance.