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- source_evidence_literature type ECO_0000212 NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_provenance.
- NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_assertion description "[To assess the prevalence of different forms of OCA and different gene mutations among non-Hispanic Caucasian patients, we performed DNA sequence analysis of the four genes associated with 'classical' OCA (TYR, OCA2, TYRP1, SLC45A2), the two principal genes associated with syndromic OCA (HPS1, HPS4), and a candidate OCA gene (SILV), in 121 unrelated, unselected non-Hispanic/Latino Caucasian patients carrying the clinical diagnosis of OCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_provenance.
- NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_assertion evidence source_evidence_literature NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_provenance.
- NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_assertion SIO_000772 18463683 NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_provenance.
- NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_assertion wasDerivedFrom gad-20150221 NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_provenance.
- NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_assertion wasGeneratedBy ECO_0000203 NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP124908.RAE3R5akEcp0PvYWNcf6Z_saRtoIi9HW9GZxKoTqunUuE130_provenance.